Canonical Allele Identifier: CA1139789937
Community Standard Title: NC_000001.11:g.199050726G=
Gene: LINC01221 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.199050726G= , CM000663.2:g.199050726G= GRCh38
NC_000001.10:g.199019855G= , CM000663.1:g.199019855G= GRCh37
NC_000001.9:g.197286478G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126351.1:n.450+9054G=